in Tag: Adverse Drug Reaction  (clear all)


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Guidelines for Recall/Withdrawal of Medicines, Medical Devices and IVDs (MCC: 5.07, Nov 2015)

This is a draft guideline incorporating medical devices. Not yet finalised

Related Tags (New Search): GMP,   QMS,   IVDs,   Non-compliance,   Recall,   Recalls,   Safety,   Adverse Drug Reaction,   SRPINS,   Adverse Drug Event

POST-MARKETING REPORTING OF ADVERSE DRUG REACTIONS TO HUMAN MEDICINES IN SOUTH AFRICA (MCC: June 2017)

Post-Marketing Reporting of Adverse Drug Reactions to Human Medicines in South Africa

Related Tags (New Search): Allopathic medicines,   Complementary medicines,   Safety,   Adverse Drug Reaction,   SRPINS,   Adverse Drug Event,   Post-marketing

Post-Marketing Reporting of Adverse Drug Reactions to Human Medicinal Products in South Africa (MCC: 2.33, Sept 2016)

The document assist the reporting of adverse drug reactions (ADRs) and in the management of safety data during post-registration and post-marketing clinical trials. To confirm that you have the latest version of this document, please visit: http://www.mccza.com

Related Tags (New Search): Safety,   Adverse Drug Reaction,   Clinical trials,   Medicines

SAFETY-RELATED PACKAGE INSERT NOTIFICATIONS (SR-PINs) - (MCC: Aug 17)

Safety-related Package Insert Notifications (SR PINS) in South Africa.Circular 2.17.

Related Tags (New Search): Allopathic medicines,   Complementary medicines,   Safety,   Adverse Drug Reaction,   SRPINS,   Adverse Drug Event,   Post-marketing

Veterinary Drug Recalls (MCC: 3.10, Jan 2004)

This guideline provides information on the recall of veterinary medicines. Circular 3.10

Related Tags (New Search): Recalls,   Adverse Drug Reaction,   Adverse Drug Event,   Veterinary medicine